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6,7-DiMethoxy-1,4-phthalazinediol

Base Information
  • Chemical Name:6,7-DiMethoxy-1,4-phthalazinediol
  • CAS No.:10001-35-1
  • Molecular Formula:C10H10N2O4
  • Molecular Weight:222.19700
  • Hs Code.:
  • Mol file:10001-35-1.mol
6,7-DiMethoxy-1,4-phthalazinediol

Synonyms:6,7-Dimethoxy-1,4-phthalazinediol;

Suppliers and Price of 6,7-DiMethoxy-1,4-phthalazinediol
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 6,7-Dimethoxy-1,4-phthalazinediol
  • 500mg
  • $ 800.00
  • Medical Isotopes, Inc.
  • 6,7-Dimethoxy-1,4-phthalazinediol
  • 50 mg
  • $ 650.00
Total 6 raw suppliers
Chemical Property of 6,7-DiMethoxy-1,4-phthalazinediol
Chemical Property:
  • PSA:84.18000 
  • LogP:0.23360 
  • Solubility.:DMSO, Methanol 
Purity/Quality:

98%,99%, *data from raw suppliers

6,7-Dimethoxy-1,4-phthalazinediol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 6,7-Dimethoxy-1,4-phthalazinediol is an intermediate in the synthesis of Carbazeran (C175790), a phosphodiesterase inhibitor drug that exhibits chronictropic and inotropic effects.
Technology Process of 6,7-DiMethoxy-1,4-phthalazinediol

There total 2 articles about 6,7-DiMethoxy-1,4-phthalazinediol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrazine hydrate; In ethanol; for 0.5h; Heating;
Guidance literature:
entspr. Phthalsaeure-anhydrid, Hydrazin, EtOH, Δ;
Guidance literature:
Multi-step reaction with 3 steps
1: 41 percent / lead tetra-acetate / CH2Cl2 / 3 h / Ambient temperature
2: 98 percent / 1.5 h / 450 °C / 0.01 Torr
3: 44 percent / aq.HBr / 6 h / Heating
With lead(IV) acetate; hydrogen bromide; In dichloromethane;
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